Ве молиме користете го овој идентификатор да го цитирате или поврзете овој запис: http://hdl.handle.net/20.500.12188/30198
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dc.contributor.authorZhivkovikj, Marijaen_US
dc.contributor.authorVolkanovska Ilijevska, Cvetankaen_US
dc.contributor.authorMehmedovikj, Marijaen_US
dc.contributor.authorRadovikj, Marijaen_US
dc.date.accessioned2024-05-17T07:23:11Z-
dc.date.available2024-05-17T07:23:11Z-
dc.date.issued2022-10-13-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/30198-
dc.description.abstractIntroduction: Euglycemic diabetic ketoacidosis (EuDKA) is a rare but serious complication of sodium-glucose cotransporter 2 (SGLT2) inhibitors. We present a case of a 39 year old patient with EuDKA precipitated by empagliflozin therapy. Case report: Male patient with a history of type 2 diabetes for 7 years, on metformin, vildagliptin, gliclazide and multiple sclerosis for 2 years, on biological therapy, was treated with high doses of corticosteroids due to progression of neurological symptomatology. Because of poorly controlled diabetes with HbA1c of 12.1%, 10mg of empagliflozin was department with complaints of malaise, abdominal discomfort, loss of appetite and muscle cramps. Laboratory analysis showed glycaemia of 8,1 mmol/l, normal blood urea, creatinine, electrolytes and high levels of ketone in urine. Patient was treated with 0,9% solution of NaCl, 40mg of pantoprazole and discharged. Several hours later due to worsening of the condition patient was admitted to the intensive care unit. On admission glycaemia was 8,1 mmol/l, heart rate 130/min, arterial tension-127/66 mmHg, oxygen saturation 87%, arterial blood gases pH- 6.87, pO2- 177mmHg, pCO2- 7 mmol/l, bicarbonate-3,0 mmol/l, potassium-3,8 mmol/l, lactate-2,8 mmol/l. Therapy with intensive fluid replacement, intravenous insulin infusion, potassium chloride, bicarbonate and noradrenalin was instituted and mechanical ventilation was indicated. After patient condition gradually improved, transition to subcutaneous insulin therapy was made. Conclusion: Early identification of diabetic ketoacidosis despite euglycemia is essential for timely institution of treatment. Avoiding initiation of SGLT-2 inhibitors in volume-depleting illnesses, diminished oral intake, infection or other metabolic stressors reduces the risk for ЕuDKA .en_US
dc.language.isoenen_US
dc.publisherUniversity Clinic of Endocrinology, Diabetes and Metabolic Disorders, Medical Faculty, University “Ss. Cyril and Methodius” - Skopjeen_US
dc.subjectEuglycemic diabetic ketoacidosisen_US
dc.subjectSGLT2en_US
dc.titleSGLT2 Inhibitor–Induced Euglycemic Diabetic кetoacidosis: A Case Reporten_US
dc.typeProceeding articleen_US
dc.relation.conference6th Macedonian Congress of Endocrinology with international participation, Ohrid, 13-16 October,2022en_US
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